Cargando…
Blind-ending Bifid Ureter – A Case Report of Rare Congenital Anomaly and its Sonographic Appearance
AIM OF THE STUDY: We report a case of a blind-ending bifid ureter in a 67-year-old woman with ascites initially diagnosed with B-mode and Color Doppler ultrasonography and afterwards verified with contrast-enhanced abdominal computed tomography. A literature review of the pathogenesis, sonographic a...
Autores principales: | , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Sciendo
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9714284/ https://www.ncbi.nlm.nih.gov/pubmed/36482924 http://dx.doi.org/10.15557/jou.2022.0031 |
_version_ | 1784842189406208000 |
---|---|
author | Łyczek, Wojciech Migda, Bartosz |
author_facet | Łyczek, Wojciech Migda, Bartosz |
author_sort | Łyczek, Wojciech |
collection | PubMed |
description | AIM OF THE STUDY: We report a case of a blind-ending bifid ureter in a 67-year-old woman with ascites initially diagnosed with B-mode and Color Doppler ultrasonography and afterwards verified with contrast-enhanced abdominal computed tomography. A literature review of the pathogenesis, sonographic appearance with differential diagnoses and clinical significance is also presented and discussed. CASE DESCRIPTION: The patient was referred for an abdominal ultrasound due to enlarged abdomen circumference. Ultrasound revealed signs of chronic pancreatitis with cavernous transformation of the portal vein and large ascites resulting in bilateral pelvicalyceal system dilatation. Additionally, we have preliminarily diagnosed right-sided, dilatated blind-ending bifid ureter with associated contralateral complete duplication of the ureter and the collecting system. These findings, initially revealed with ultrasound, were confirmed with contrast-enhanced abdominal computed tomography. CONCLUSIONS: To our knowledge, this is the first detailed description of sonographic appearance of blind-ending bifid ureter. |
format | Online Article Text |
id | pubmed-9714284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Sciendo |
record_format | MEDLINE/PubMed |
spelling | pubmed-97142842022-12-07 Blind-ending Bifid Ureter – A Case Report of Rare Congenital Anomaly and its Sonographic Appearance Łyczek, Wojciech Migda, Bartosz J Ultrason Case-Report AIM OF THE STUDY: We report a case of a blind-ending bifid ureter in a 67-year-old woman with ascites initially diagnosed with B-mode and Color Doppler ultrasonography and afterwards verified with contrast-enhanced abdominal computed tomography. A literature review of the pathogenesis, sonographic appearance with differential diagnoses and clinical significance is also presented and discussed. CASE DESCRIPTION: The patient was referred for an abdominal ultrasound due to enlarged abdomen circumference. Ultrasound revealed signs of chronic pancreatitis with cavernous transformation of the portal vein and large ascites resulting in bilateral pelvicalyceal system dilatation. Additionally, we have preliminarily diagnosed right-sided, dilatated blind-ending bifid ureter with associated contralateral complete duplication of the ureter and the collecting system. These findings, initially revealed with ultrasound, were confirmed with contrast-enhanced abdominal computed tomography. CONCLUSIONS: To our knowledge, this is the first detailed description of sonographic appearance of blind-ending bifid ureter. Sciendo 2022-09-01 /pmc/articles/PMC9714284/ /pubmed/36482924 http://dx.doi.org/10.15557/jou.2022.0031 Text en © 2022 Wojciech Łyczek et al., published by Sciendo https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. |
spellingShingle | Case-Report Łyczek, Wojciech Migda, Bartosz Blind-ending Bifid Ureter – A Case Report of Rare Congenital Anomaly and its Sonographic Appearance |
title | Blind-ending Bifid Ureter – A Case Report of Rare Congenital Anomaly and its Sonographic Appearance |
title_full | Blind-ending Bifid Ureter – A Case Report of Rare Congenital Anomaly and its Sonographic Appearance |
title_fullStr | Blind-ending Bifid Ureter – A Case Report of Rare Congenital Anomaly and its Sonographic Appearance |
title_full_unstemmed | Blind-ending Bifid Ureter – A Case Report of Rare Congenital Anomaly and its Sonographic Appearance |
title_short | Blind-ending Bifid Ureter – A Case Report of Rare Congenital Anomaly and its Sonographic Appearance |
title_sort | blind-ending bifid ureter – a case report of rare congenital anomaly and its sonographic appearance |
topic | Case-Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9714284/ https://www.ncbi.nlm.nih.gov/pubmed/36482924 http://dx.doi.org/10.15557/jou.2022.0031 |
work_keys_str_mv | AT łyczekwojciech blindendingbifidureteracasereportofrarecongenitalanomalyanditssonographicappearance AT migdabartosz blindendingbifidureteracasereportofrarecongenitalanomalyanditssonographicappearance |